Green Chemistry · 2012 · 36 citations · 33 references
Diastereoselective ConstructionChemical EngineeringDiversity Oriented SynthesisPictet–spengler ReactionEngineeringNatural SciencesDiversity-oriented SynthesisOrganic ChemistryCatalysisChemistryNatural Product SynthesisAsymmetric CatalysisEnvironment-friendly High-yielding MethodSynthetic ChemistryEnantioselective SynthesisIndole Alkaloids
An environment-friendly high-yielding method for the racemic and asymmetric diastereoselective preparation of indole alkaloids via Pictet–Spengler reaction is reported. The reaction proceeds with short reaction times under solvent-free and microwave-irradiation conditions.
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THE VINCA ALKALOIDS: A NEW CLASS OF ONCOLYTIC AGENTS.
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Quinolizinone Products, Engineering, H-bond Donor Catalysis +14
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Enantioselective Pictet-spengler Reaction, Engineering, Natural Sciences +11